A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560076



Internal ID16347485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:106247520..106248184hg38UCSC Ensembl
Innerchr12:106641298..106641962hg19UCSC Ensembl
Innerchr12:105165428..105166092hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38665
hg19665
hg18665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2849n54
Supporting Variantsnssv801879
Samples
Known GenesCKAP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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